SCHEMBL355890

SCHEMBL355890

BC(CSC(C)(C)C)SC(C)(C)C

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL15907977 0.70
SCHEMBL6889646 0.69
SCHEMBL19542976 0.68
SCHEMBL12139950 0.65
Ammonia Solution, Strong SCHEMBL7247171 0.63 HTR1A (0.32)
SCHEMBL20034838 0.63 HTR1A (0.32)
SCHEMBL20034983 0.61 HTR1A (0.31)
SCHEMBL8744971 0.61
SCHEMBL19293395 0.61
SCHEMBL16284415 0.61

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 60 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1899317-A2 ENANTIOMERS OF N,N-DIMETHYL-3-(2-THIENYL)-3-HYDROXYPROPANAMINE BORANE AS INTERMEDIATES IN THE SYNTHESIS OF DULOXETINE Teva Pharmaceutical Industries Ltd (IL) 2008-03-19 EP claimed
US-20080015362-A1 Process for the preparation of optically active (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine TEVA PHARMACEUTICALS USA, INC. 2008-01-17 US claimed
WO-2007123900-A2 ENANTIOMERS OF N,N-DIMETHYL-3-(2-THIENYL)-3-HYDROXYPROPANAMINE BORANE AS INTERMEDIATES IN THE SYNTHESIS OF DULOXETINE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-11-01 WO claimed
WO-2023228980-A1 PRODUCTION METHOD FOR FLUOROPOLYETHER GROUP–CONTAINING COMPOUND ダイキン工業株式会社 2023-11-30 WO disclosed
US-11723900-B2 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compounds THERAVANCE BIOPHARMA R&D IP, LLC (US) 2023-08-15 US disclosed
US-20220087995-A1 4-[2-(2-FLUOROPHENOXYMETHYL)PHENYL]PIPERIDINE COMPOUNDS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2022-03-24 US disclosed
US-10946007-B2 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compounds THERAVANCE BIOPHARMA R&D IP, LLC (US) 2021-03-16 US disclosed
US-20200316048-A1 4-[2-(2-FLUOROPHENOXYMETHYL)PHENYL]PIPERIDINE COMPOUNDS THERAVANCE BIOPHARMA R&D IP, LLC (US) 2020-10-08 US disclosed
US-10722504-B2 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compounds THERAVANCE BIOPHARMA R&D IP, LLC (US) 2020-07-28 US disclosed
US-10441579-B2 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compounds THERAVANCE BIOPHARMA R&D IP, LLC (US) 2019-10-15 US disclosed
EP-2358675-B9 4-[2-(2-Fluorophenoxymethyl)phenyl]piperidine compounds THERAVANCE INC (US) 2019-09-11 EP disclosed
US-20090318720-A1 Process for selectively synthesising 3 alpha-hydroxychlormadinone acetate GRUNENTHAL GMBH (DE) 2009-12-24 US disclosed
EP-2114862-A1 PROCESS FOR THE PREPARATION OF O-DESMETHYL VENLAFAXINE Merck Generics (UK) Limited (GB) 2009-11-11 EP disclosed
WO-2008093142-A1 PROCESS FOR THE PREPARATION OF O-DESMETHYL VENLAFAXINE GENERICS [UK] LIMITED (GB) 2008-08-07 WO disclosed
EP-1899317-A2 ENANTIOMERS OF N,N-DIMETHYL-3-(2-THIENYL)-3-HYDROXYPROPANAMINE BORANE AS INTERMEDIATES IN THE SYNTHESIS OF DULOXETINE Teva Pharmaceutical Industries Ltd (IL) 2008-03-19 EP disclosed
US-20080015362-A1 Process for the preparation of optically active (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine TEVA PHARMACEUTICALS USA, INC. 2008-01-17 US disclosed
WO-2007123900-A2 ENANTIOMERS OF N,N-DIMETHYL-3-(2-THIENYL)-3-HYDROXYPROPANAMINE BORANE AS INTERMEDIATES IN THE SYNTHESIS OF DULOXETINE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-11-01 WO disclosed
US-20060241298-A1 Methods for synthesis of dicarbamate compounds and intermediates in the formation thereof MEDPOINTE HEALTHCARE INC. 2006-10-26 US disclosed
EP-1582250-A2 Absorbent with improved ocidation resistance and process for deacidifying fluid fluxes BASF AKTIENGESELLSCHAFT (DE) 2005-10-05 EP disclosed
US-20050202967-A1 an aliphatic amine, in particular an alkanolamine, and a non-hydroquinoid antioxidant for removal of CO2, H2S, SO2, CS2, HCN, COS, disulfides or mercaptans as impurities in reaction gases formed in the oxidation of organic materials to prevent the emission of above gases BASF AKTIENGESELLSCHAFT (DE) 2005-09-15 US disclosed